NDC 71839-122 – Pantoprazole sodium
Pantoprazole Sodium 40 mg/10mL · Injection, Powder, For Solution · Intravenous
Product NDC71839-122
Product details
- Brand name
- Pantoprazole sodium
- Generic name
- Pantoprazole sodium
- Labeler
- BE Pharmaceuticals Inc.
- Dosage form
- Injection, Powder, For Solution
- Route
- Intravenous
- Marketing category
- ANDA · ANDA216171
- Marketed since
- May 25, 2022
- Listing expires
- December 31, 2026
- Pharmacologic class
- Proton Pump Inhibitor
Active ingredients
- Pantoprazole Sodium 40 mg/10mL
Uses, dosage, side effects and warnings for Pantoprazole Sodium →
Package NDC codes (3)
| Package NDC | Description | Since |
|---|---|---|
| 71839-122-01 | 1 VIAL in 1 CARTON (71839-122-01) / 10 mL in 1 VIAL | May 25, 2022 |
| 71839-122-10 | 10 CARTON in 1 PACKAGE (71839-122-10) / 1 VIAL in 1 CARTON / 10 mL in 1 VIAL | May 25, 2022 |
| 71839-122-25 | 25 CARTON in 1 PACKAGE (71839-122-25) / 1 VIAL in 1 CARTON / 10 mL in 1 VIAL | May 25, 2022 |
Recalls mentioning this NDC
- D-1148-2023 Sep 20, 2023 · Class II
Lack of Assurance of Sterility: Powder discoloration due to small crack in some vials.
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